Abstract A032: Efficacy of nuclear envelope protein targeting CAR T cell therapy for MYC driven group 3 medulloblastoma

Abstract Medulloblastoma (MB) is the most common, malignant pediatric brain tumour comprised of four distinct molecular subgroups (WNT, SHH, Group 3, and Group 4). A subset of Group 3 MB tumors harbor focal amplifications of the MYC oncogene (MYC-G3MB) that are prone to leptomeningeal spread and recurrence which remains incurable. Therefore, there is an urgent need for the development of therapeutic modalities that are safe and have potent antitumour efficacy against recurrent MB. We discovered that nuclear envelope (NE) proteins LBR and TMPO are aberrantly presented to the cell surface in MYC-G3MB cell lines with little to no expression in normal cells. We identified that positive LBR staining in MB patient samples correlated with a significantly worse prognosis and was also enriched in recurrent tissue compared to their matched primary samples. High resolution microscopy of endogenously tagged HALO-LBR and mNeon-TMPO reveals cell surface presentation to be linked to ER or ER-like vesicles that are trafficked and accumulated at the cell surface. Transcriptomic analysis of LBR cell surface positive and negative cells identified that cell surface positivity is significantly linked to cell division and mitotic processes. Tracking of LBR and TMPO expression across embryonal development identify expression to be significantly linked to prenatal development that dampens postnatally. To generate NE-specific CAR T cell therapies that would target these hyper proliferative specific G3MB subpopulations we engineered single domain antibodies (sdAb) against the N-termini of LBR and TMPO. NE protein targeting CAR T cell therapies revealed potent antitumour efficacy against MYC-G3MB cells both in vivo and in vitro. We present a novel class of therapeutic targets that define a mechanistically distinct therapy-resistant population for potential translation into early phase clinical trials. Citation Format: Yujin Suk, Jorge Ibañez-Vega, Martin Rossotti, Vaseem Shaikh, Yiyun Chen, Hardikkumar Patel, Laura Escudero, Alberto Delaidelli, Sarah Slassi, Carlos B. Bazan, Aapti Khanna, Sumayyah Sokeechand, Erika Apel, Iqra Chaudhry, Stefan Custers, Shan Grewal, Mohamed Taleb, Takuma Nakashima, William Maich, Lucas Asselstine, Dillon McKenna, Minomi Subapanditha, Petar Miletic, Yuxi Xiao, William D. Gwynne, Jason Moffat, Hiromichi Suzuki, Poul Sorensen, Ray Truant, Kevin A. Henry, Elena Sotillo, Chitra Venugopal, Crystal Mackall, Giedre Krenciute, Sheila K. Singh. Efficacy of nuclear envelope protein targeting CAR T cell therapy for MYC driven group 3 medulloblastoma [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Brain Cancer; 2026 Mar 23-25; Philadelphia, PA. Philadelphia (PA): AACR; Cancer Res 2026;86(6_Suppl):Abstract nr A032.

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Journal
Cancer Research
Published
2026-03-23
DOI
https://doi.org/10.1158/1538-7445.brain26-a032
Primary Topic
CAR-T cell therapy research
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article
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article

Abstract A032: Efficacy of nuclear envelope protein targeting CAR T cell therapy for MYC driven group 3 medulloblastoma

Sheila Kumari Singh, Martín A. Rossotti, Laura Escudero, Shan Grewal et al.
Cancer Research
CAR-T cell therapy research
article

Abstract A032: Efficacy of nuclear envelope protein targeting CAR T cell therapy for MYC driven group 3 medulloblastoma

Sheila Kumari Singh, Martín A. Rossotti, Laura Escudero, Shan Grewal, Ray Truant, Yuxi Xiao, Alberto Delaidelli, Dillon McKenna, Jorge Ibañez-Vega, William D. Gwynne, Stefan Custers, Iqra Chaudhry, Vaseem Shaikh, Minomi Subapanditha, Takuma Nakashima, William Maich, Petar Miletic, Kevin A. Henry, Giedre Krenciute, Yujin Suk, Hiromichi Suzuki, J. W. Moffat, P.H.B. Sorensen, Carlos Bazan, Erika Apel, Sarah Slassi, Lucas Asselstine, Yiyun Chen, Mohamed Taleb, Sumayyah Sokeechand, Elena Sotillo, Hardikkumar Patel, Aapti Khanna, Crystal Mackall, Chitra Venugopal
article en

Abstract

Abstract Medulloblastoma (MB) is the most common, malignant pediatric brain tumour comprised of four distinct molecular subgroups (WNT, SHH, Group 3, and Group 4). A subset of Group 3 MB tumors harbor focal amplifications of the MYC oncogene (MYC-G3MB) that are prone to leptomeningeal spread and recurrence which remains incurable. Therefore, there is an urgent need for the development of therapeutic modalities that are safe and have potent antitumour efficacy against recurrent MB. We discovered that nuclear envelope (NE) proteins LBR and TMPO are aberrantly presented to the cell surface in MYC-G3MB cell lines with little to no expression in normal cells. We identified that positive LBR staining in MB patient samples correlated with a significantly worse prognosis and was also enriched in recurrent tissue compared to their matched primary samples. High resolution microscopy of endogenously tagged HALO-LBR and mNeon-TMPO reveals cell surface presentation to be linked to ER or ER-like vesicles that are trafficked and accumulated at the cell surface. Transcriptomic analysis of LBR cell surface positive and negative cells identified that cell surface positivity is significantly linked to cell division and mitotic processes. Tracking of LBR and TMPO expression across embryonal development identify expression to be significantly linked to prenatal development that dampens postnatally. To generate NE-specific CAR T cell therapies that would target these hyper proliferative specific G3MB subpopulations we engineered single domain antibodies (sdAb) against the N-termini of LBR and TMPO. NE protein targeting CAR T cell therapies revealed potent antitumour efficacy against MYC-G3MB cells both in vivo and in vitro. We present a novel class of therapeutic targets that define a mechanistically distinct therapy-resistant population for potential translation into early phase clinical trials. Citation Format: Yujin Suk, Jorge Ibañez-Vega, Martin Rossotti, Vaseem Shaikh, Yiyun Chen, Hardikkumar Patel, Laura Escudero, Alberto Delaidelli, Sarah Slassi, Carlos B. Bazan, Aapti Khanna, Sumayyah Sokeechand, Erika Apel, Iqra Chaudhry, Stefan Custers, Shan Grewal, Mohamed Taleb, Takuma Nakashima, William Maich, Lucas Asselstine, Dillon McKenna, Minomi Subapanditha, Petar Miletic, Yuxi Xiao, William D. Gwynne, Jason Moffat, Hiromichi Suzuki, Poul Sorensen, Ray Truant, Kevin A. Henry, Elena Sotillo, Chitra Venugopal, Crystal Mackall, Giedre Krenciute, Sheila K. Singh. Efficacy of nuclear envelope protein targeting CAR T cell therapy for MYC driven group 3 medulloblastoma [abstract]. In: Proceedings of the AACR Special Conference in Cancer Research: Brain Cancer; 2026 Mar 23-25; Philadelphia, PA. Philadelphia (PA): AACR; Cancer Res 2026;86(6_Suppl):Abstract nr A032.

Cancer ResearchVol. 86(6_Supplement)
St. Jude Children's Research Hospital (US), University of British Columbia (CA), Palo Alto University (US), University of Toronto (CA), The Cancer Institute Hospital (JP), National Research Council Canada (CA), Mass General Brigham (US), National Cancer Research Institute (GB), Stanford University (US), McMaster University (CA)
Good health and well-being
Openalex Percentile: Top 11%
CAR-T cell therapy research
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